Canonical Allele Identifier: CA2799081318

Gene: HTR2A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.46892910C>A , CM000675.2:g.46892910C>A	GRCh38
NC_000013.10:g.47467045C>A , CM000675.1:g.47467045C>A	GRCh37
NC_000013.9:g.46365046C>A	NCBI36
NG_013011.1:g.9125G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542664.4:c.413-320G>T MANE Select	ENSP00000437737.1:n.413-320G>T
ENST00000543956.5:c.-77-320G>T	ENSP00000441861.2:n.-77-320G>T
ENST00000378688.8:c.413-320G>T	ENSP00000367959.3:n.413-320G>T
ENST00000542664.3:c.413-320G>T	ENSP00000437737.1:n.413-320G>T
ENST00000543956.4:c.161-320G>T	ENSP00000441861.1:n.161-320G>T
NM_000621.4:c.413-320G>T	NP_000612.1:n.413-320G>T
NM_001165947.2:c.161-320G>T	NP_001159419.1:n.161-320G>T
NM_000621.5:c.413-320G>T MANE Select	NP_000612.1:n.413-320G>T
NM_001165947.5:c.-77-320G>T	NP_001159419.2:n.-77-320G>T
NM_001378924.1:c.413-320G>T	NP_001365853.1:n.413-320G>T